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2932-48-1

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2932-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2932-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2932-48:
(6*2)+(5*9)+(4*3)+(3*2)+(2*4)+(1*8)=91
91 % 10 = 1
So 2932-48-1 is a valid CAS Registry Number.

2932-48-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(phenyl)azanium,hexafluorophosphate

1.2 Other means of identification

Product number -
Other names Benzenaminium,N,N,N-trimethyl-,hexafluorophosphate(1-)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2932-48-1 SDS

2932-48-1Downstream Products

2932-48-1Relevant articles and documents

Design and synthesis of a task-specific ionic liquid as a transducer in potentiometric sensors

Ping, Jianfeng,Wang, Yixian,Ying, Yibin,Wu, Jian

, p. 19782 - 19784 (2013)

A task-specific ionic liquid called N,N,N-trimethylaniline hexafluorophosphate was synthesized and further employed as an ion-to-electron transducer in potentiometric sensors with excellent performance. The Royal Society of Chemistry 2013.

Effects of Quaternary Ammonium Salts on Reactions of Aromatic radical Anions Formed in Tetrahydrofuran by Pulse Radiolysis

Yamamoto, Yukio,Nishida, Shoichi,Yabe, Katsuyoshi,Hayashi, Koichiro,Takeda,Seishi,Tsumori, Kunihiko

, p. 2368 - 2372 (2007/10/02)

Pulse radiolysis of biphenyl (BP) and pyrene (Py) in tetrahydrofuran (THF) solution was carried out in the presence of various kinds of quaternary ammonium salts, such as Bu4NPF6, Bu4NBF4, Bu4NI, BzMe3NPF6 and PhMe3NPF6 (Bu, butyl; Me, mthyl; Bz, benzyl; and Ph, phenyl).The decay behaviors of the radical anions, BP-. and Py-., are significantly affected by the addition of the salts.The anions of the salts, PF6-, BF4-, and I-, are considered to form ion pairs with the solvent counterions, THF(H+), resulting in a retardation of the neutralization reactions.The rate constants for the neutralization reactions have been determined in the absence and presence of Bu4NPF6.The addition of BzMe3NPF6 (or PhMe3NPF6) accelerates the decay of BP-. and retards the decay of Py-., depending on the rates of reactions of the radical anions with BzMe3N+ (or PhMe3N+).The reactivity of BP-. in the electron transfer to Py seems to be reduced in the presence of Bu4NPF6.The effect of Bu4N+ on the reactions of the radical anions is discussed.

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